ArticleDiagnostics (Basel, Switzerland)2022
Computer-Aided Assessment of Melanocytic Lesions by Means of a Mitosis Algorithm.
Article in Diagnostics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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9 citing papers in PubMed, 12 citations in OpenAlex.
- Artificial Intelligence in Dermatopathology: An Update and Review of the Current Literature.Diagnostics (Basel, Switzerland) · 2026Review
- Large-Scale Dermatopathology Dataset for Lesion Segmentation: Model Development and Analysis.Journal of Korean medical science · 2025Article
- Current Trends and Future Directions of Digital Pathology and Artificial Intelligence in Dermatopathology: A Scientometric-Based Review.Diagnostics (Basel, Switzerland) · 2025Review
- Machine learning to detect melanoma exploiting nuclei morphology and Spatial organization.Scientific reports · 2025Article
- Mini review on skin biopsy: traditional and modern techniques.Frontiers in medicine · 2025Review
- Artificial Intelligence in Digital Pathology for Bladder Cancer: Hype or Hope? A Systematic Review.Cancers · 2023Review
- Recent Advances in Melanoma Diagnosis and Prognosis Using Machine Learning Methods.Current oncology reports · 2023Review
- Review
- Diagnostic and Prognostic Deep Learning Applications for Histological Assessment of Cutaneous Melanoma.Cancers · 2022Review
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Authors and funding
10 authors at 7 institutions in 3 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
An increasing number of pathology laboratories are now fully digitised, using whole slide imaging (WSI) for routine diagnostics. WSI paves the road to use artificial intelligence (AI) that will play an increasing role in computer-aided diagnosis (CAD). In melanocytic skin lesions, the presence of a dermal mitosis may be an important clue for an intermediate or a malignant lesion and may indicate worse prognosis. In this study a mitosis algorithm primarily developed for breast carcinoma is applied to melanocytic skin lesions. This study aimed to assess whether the algorithm could be used in diagnosing melanocytic lesions, and to study the added value in diagnosing melanocytic lesions in a practical setting. WSI's of a set of hematoxylin and eosin (H&E) stained slides of 99 melanocytic lesions (35 nevi, 4 intermediate melanocytic lesions, and 60 malignant melanomas, including 10 nevoid melanomas), for which a consensus diagnosis was reached by three academic pathologists, were subjected to a mitosis algorithm based on AI. Two academic and six general pathologists specialized in dermatopathology examined the WSI cases two times, first without mitosis annotations and after a washout period of at least 2 months with mitosis annotations based on the algorithm. The algorithm indicated true mitosis in lesional cells, i.e., melanocytes, and non-lesional cells, i.e., mainly keratinocytes and inflammatory cells. A high number of false positive mitosis was indicated as well, comprising melanin pigment, sebaceous glands nuclei, and spindle cell nuclei such as stromal cells and neuroid differentiated melanocytes. All but one pathologist reported more often a dermal mitosis with the mitosis algorithm, which on a regular basis, was incorrectly attributed to mitoses from mainly inflammatory cells. The overall concordance of the pathologists with the consensus diagnosis for all cases excluding nevoid melanoma (
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